1-(2-(2-methyl-5-nitro-1H-imidazol-1-yl)ethyl)-1H-benzo[d]imidazole | 321979-82-2

• 分子结构分类: 有机化合物 - 有机杂环化合物 - 苯并咪唑类
• 英文名称: 1-(2-(2-methyl-5-nitro-1H-imidazol-1-yl)ethyl)-1H-benzo[d]imidazole
• 英文别名: 1-(2-(2-methyl-5-nitro-1H-imidazol-1-yl)ethyl)-1H-benzimidazole；1-[2-(2-Methyl-5-nitroimidazol-1-yl)ethyl]benzimidazole
• CAS: 321979-82-2
• 化学式: C₁₃H₁₃N₅O₂
• 分子量: 271.279
• InChiKey: NFZQHWPKNNVTCA-UHFFFAOYSA-N

计算性质

• 辛醇/水分配系数(LogP)：
  1.7
• 重原子数：
  20
• 可旋转键数：
  3
• 环数：
  3.0
• sp3杂化的碳原子比例：
  0.23
• 拓扑面积：
  81.5
• 氢给体数：
  0
• 氢受体数：
  4

反应信息

• 作为产物：
  描述：

  甲硝唑 在 吡啶 、 potassium carbonate 作用下， 以 氯仿 、 N,N-二甲基甲酰胺 为溶剂， 反应 48.0h， 生成 1-(2-(2-methyl-5-nitro-1H-imidazol-1-yl)ethyl)-1H-benzo[d]imidazole
  参考文献：
  名称：

  甲硝唑芳氧基，羧基和吡咯衍生物：合成，抗肿瘤活性，QSAR，分子对接和动力学研究

  摘要：

  已经合成了一系列新颖的甲硝唑芳氧基，羧基和唑衍生物，并通过MTT分析评估了它们对三种癌细胞系的细胞毒活性。化合物4m，4l和4d表现出最强的细胞毒活性（IC 50小于100 µg / mL）。还通过流式细胞术检测了这些化合物的凋亡。进行了对接研究以提出可能的靶蛋白。下一步，对与化合物4m结合的拟议目标蛋白粘着斑激酶（FAK，PDB代码：2ETM）进行了分子动力学模拟。As，4m 提示其具有强力的细胞毒活性和可接受的凋亡作用，它可能是潜在的抗癌候选药物，可以通过抑制FAK发挥作用。

  DOI：

  10.1016/j.bmc.2018.12.003

文献信息

• Imidazole derivatives as possible microbicides with dual protection
  作者：Lalit Kumar、Amit Sarswat、Nand Lal、Vishnu L. Sharma、Ashish Jain、Rajeev Kumar、Vikas Verma、Jagdamba P. Maikhuri、Awanit Kumar、Praveen K. Shukla、Gopal Gupta

  DOI：10.1016/j.ejmech.2009.10.021

  日期：2010.2

  Twenty seven derivatives (2-28) of 2-(2-methyl-5-nitro-1H-imidazol-1-yl)ethanol were synthesized and evaluated for anti-trichomonas, spermicidal and antifungal activities. Twenty six compounds were active against Trichomonas vaginalis at MIC ranging from 1-42 mu M and seven compounds (9,18,19,22,24,26,28) immobilized 100% human spermatozoa at 1% concentration (w/v). Twenty three compounds (2,3,5,8-26,28) exhibited antifungal activity at 25-50 mu g/mL concentration. Seven compounds (9,18,19,22,24,26,28) showed significant anti-trichomonas and spermicidal activities and also exhibited mild antifungal activity. All the compounds were highly safe towards human cervical cell line (HeLa) as shown by the cell-viability assay of HeLa cells at 200 mu g/mL concentration, whereas nonoxynol-9 (N-9, the marketed spermicidal microbicide) was highly cytotoxic. Therefore, it may be concluded that introduction of the pharmacophore responsible for spermicidal activity into a proven anti-trichomonas structure may lead to a potent dual function microbicide better and safer than N-9. (C) 2009 Elsevier Masson SAS. All rights reserved.